Expanding the phenotypic spectrum of mutations in LRP2: a novel candidate gene of non-syndromic familial comitant strabismus

BACKGROUND: Comitant strabismus (CS) is a heterogeneous disorder that is a major contributing factor to unilateral childhood-onset visual impairment. Studies have confirmed that genetic factors play an important role in the development of CS. The aim of this study was to identify the genetic cause o...

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Detalles Bibliográficos
Autores principales: Wang, Yue, Chen, Xuejuan, Jiang, Tao, Gu, Yayun, Zhang, Xiaohan, Yuan, Wenwen, Zhao, Andi, Li, Rui, Wang, Zijin, Hu, Zhibin, Liu, Hu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647414/
https://www.ncbi.nlm.nih.gov/pubmed/34872573
http://dx.doi.org/10.1186/s12967-021-03155-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8647414/
https://www.ncbi.nlm.nih.gov/pubmed/34872573
http://dx.doi.org/10.1186/s12967-021-03155-z

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